@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_head {
  this: np:hasAssertion dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_assertion;
    np:hasProvenance dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_provenance;
    np:hasPublicationInfo dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_assertion a np:Assertion .
  
  dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_provenance a np:Provenance .
  
  dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_assertion {
  miriam-gene:4513 a ncit:C16612 .
  
  lld:C0268237 a ncit:C7057 .
  
  dgn-gda:DGN894ad564aece6b2b81b34a1400eeb7a1 sio:SIO_000628 miriam-gene:4513, lld:C0268237;
    a sio:SIO_001121 .
}

dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_provenance {
  dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_assertion dcterms:description
      "[The accumulation of H(2)S over time causes progressive COX deficiency in animal tissues and human cells, which is associated with reduced amount of COX holoenzyme, and of several COX subunits, including mitochondrially encoded cytochrome c oxidase 1 (MTCO1), MTCO2, COX4, and COX5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:20812865;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP406181.RAqPjfnlNOhmcD0rwmM4Ab4-O7vq75QR5nvCNWtkPRcpM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}